CN108329496B - 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法 - Google Patents

一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法 Download PDF

Info

Publication number
CN108329496B
CN108329496B CN201810144941.0A CN201810144941A CN108329496B CN 108329496 B CN108329496 B CN 108329496B CN 201810144941 A CN201810144941 A CN 201810144941A CN 108329496 B CN108329496 B CN 108329496B
Authority
CN
China
Prior art keywords
chitosan oligosaccharide
graphene oxide
silver
rubber material
preparation
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
CN201810144941.0A
Other languages
English (en)
Other versions
CN108329496A (zh
Inventor
张�杰
卫爱丽
李伟
郑少明
管路遥
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Taiyuan University of Technology
Original Assignee
Taiyuan University of Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taiyuan University of Technology filed Critical Taiyuan University of Technology
Priority to CN201810144941.0A priority Critical patent/CN108329496B/zh
Publication of CN108329496A publication Critical patent/CN108329496A/zh
Application granted granted Critical
Publication of CN108329496B publication Critical patent/CN108329496B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/12Chemical modification
    • C08J7/14Chemical modification with acids, their salts or anhydrides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2307/00Characterised by the use of natural rubber
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/08Metals
    • C08K2003/0806Silver
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • C08K3/042Graphene or derivatives, e.g. graphene oxides
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/10Encapsulated ingredients

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials For Medical Uses (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

本发明公开了一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法,该方法包括如下步骤:1)壳寡糖包裹纳米银的制备;2)天然橡胶表面改性;3)在天然橡胶表面进行的壳寡糖包裹纳米银和氧化石墨烯的层层自组装:将壳寡糖包裹纳米银溶液和氧化石墨烯溶液中分别交替自组装多次后,得到壳寡糖包裹纳米银为最外层的含多个双分子层的表面层层自组装修饰的天然胶乳膜片,洗涤,干燥,得到生物多糖自组装修饰的壳聚糖抗菌生物材料。该方法制备的医用天然橡胶材料具有优异的抗菌活性,且制备过程简单,易于控制,制备条件温和,成本低廉。

Description

一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制 备方法
技术领域
本发明涉及一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法,属于医用抗菌橡胶材料及其制备技术领域。
背景技术
在临床治疗中,有些病人需要长期在体内留置介入性导管。在人体环境中介入性导管容易滋生细菌,引起严重的细菌感染。细菌粘附在导管表面并迅速生长繁殖,一段时间以后大量细菌黏附在一起形成一层生物膜。这层生物膜为细菌提供生存环境,并阻挡外来药物进入,危及病人生命安全。因此,对介入性导管进行抗菌改性,降低感染风险逐渐成为研究热点。
天然胶乳(橡胶)是制作介入导管的常用原料,但天然胶乳本身不具有抗菌性,必须对其进行抗菌改性。
导管植入人体后只有表面部分与人体接触,因此可以仅对导管表面进行改性。
发明内容
本发明旨在提供一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法,该方法将壳寡糖包裹纳米银和氧化石墨烯交替组装在橡胶表面,形成层层自组装结构。该方法制备过程简单,易于控制,制备条件温和,成本低廉。
本发明在导管表面接枝抗菌剂,以化学键、氢键或静电力将导管与抗菌剂紧密结合形成抗菌涂层,或在基体加工时蘸取适量液体抗菌剂。这种方法成本低,工艺简单,适用范围广,能最大程度的发挥抗菌剂作用。
本发明提供了一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,包括以下步骤:
(1)壳寡糖包裹纳米银的制备:
(2)天然橡胶表面改性:在天然橡胶表面进行壳寡糖包裹纳米银和氧化石墨烯的层层自组装:将壳寡糖包裹纳米银溶液和氧化石墨烯溶液中分别交替自组装多次后,得到壳寡糖包裹纳米银为最外层的含多个双分子层的表面层层自组装修饰的天然胶乳膜片,洗涤,干燥,得到壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料。
上述制备方法具体包括以下步骤:
(1)壳寡糖包裹纳米银的制备
将0.1%wt硝酸银溶液与0.1%wt壳寡糖溶液按体积比为5~30:70~95加入搅拌器中,室温下搅拌0.5-1h,混合溶液置于4mL石英比色皿中,通氮气10s-30s除尽空气并密封,将石英比色皿置于240-290nm紫外灯3-8cm处照射5min-30min,紫外灯功率10-40W;
混合溶液加入相同体积的无水乙醇在13000r/min-15000r/min转速下离心30min-80min取沉淀,并用50%wt乙醇离心洗涤两次并冷冻干燥,即得到壳寡糖包裹纳米银复合抗菌剂CS-AgNPs粉末;壳寡糖包裹纳米银复合抗菌剂粉末溶于水,并超声20-30min,即得壳寡糖包裹纳米银分散液;
所述硝酸银被还原后是单质银。
(2)天然橡胶(NR)表面处理
去离子水清洗后的天然橡胶胶片在80%-98%浓硫酸下浸泡5-10min,取出用去离子水清洗3-7次;
(3)在天然橡胶(NR)表面进行的壳寡糖纳米银和氧化石墨烯层层自组装
将上述步骤(2)得到的天然橡胶基材加入到浓度为0.5mg/mL-2 mg/mL氧化石墨烯溶液中浸泡30-60min,然后分离出膜片用超纯水溶液洗涤4-6次,制备出表面具有氧化石墨烯的橡胶膜片;再将膜片加入步骤(1)得到的壳寡糖包裹纳米银分散液中浸泡30-60min,分离出膜片用超纯水溶液洗涤4-6次,完成基材表面的第一个双分子层自组装;重复上述过程,在壳寡糖包裹纳米银溶液和氧化石墨烯溶液中分别交替自组装3-5次后,得到壳寡糖包裹纳米银为最外层的表面层层自组装修饰的医用橡胶材料。
上述制备方法中,所述壳寡糖的分子量为1000-10000。
上述制备方法中,所述的氧化石墨烯为微米级,其直径为0.7-1.2 nm微米,单层率(是指氧化石墨烯中为单层的个数)大于95%。
本发明还提供了上述制备方法制得的表面层层自组装修饰的医用橡胶材料。
本发明所述的表面层层自组装修饰的医用橡胶材料,含有2~10层的层状结构。
本方法所制备的壳寡糖包裹纳米银/氧化石墨烯层层自组装修饰的医用天然橡胶材料,经平板菌落计数法试验检测对大肠杆菌和金色葡萄球菌抑菌率达到100%。
本发明的有益效果:
本发明制备方法操作简便,快捷,排除了有毒化学试剂的使用,保障了人身的健康,可安全地用于可广泛用于医疗、卫生等领域。
附图说明
图1是实施例1和3壳寡糖包裹纳米银/氧化石墨烯层层修饰的医用橡胶材料的SEM图。其中a为组装一次的图,b为组装五次的图。
图2为实施例1~3所得产品的抑菌环测试效果图。
具体实施方式
下面通过实施例来进一步说明本发明,但不局限于以下实施例。
实施例1:
本实施例提供一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,包括以下步骤:
(1)将0.1%wt的硝酸银水溶液与0.1%wt 的壳寡糖水溶液按体积比为10:90加入搅拌器,室温下均匀搅拌10min;将上述混合溶液置于4mL比色皿中,通氮气20s除尽空气并密封;将上述容器置于距紫外灯5cm处照射30min,紫外灯波长为272nm,紫外灯功率为20w;将混合溶液透析纯化即得壳寡糖纳米银复合抗菌剂;
(2)去离子水清洗后的天然橡胶胶片在80%浓硫酸下浸泡15min,取出用去离子水清洗4次;
(3)将上述步骤(2)得到天然橡胶基材加入到氧化石墨烯溶液(1.0mg/mL-1)中浸泡10min,然后分离出膜片用超纯水溶液洗涤5次,制备出表面具有氧化石墨烯的CS-AgNPs/GO膜片;再将CS-AgNPs/GO膜片加入壳寡糖包裹纳米银中浸泡10min分钟,分离出膜片用超纯水溶液洗涤5次,完成基材表面的第一个双分子层自组装;重复上述过程,在壳寡糖包裹纳米银溶液和氧化石墨烯溶液中分别交替自组装1次后,得到含有4层的壳寡糖包裹纳米银为最外层的医用橡胶膜片。
图1示出了本实施例壳寡糖包裹纳米银/氧化石墨烯层层修饰的医用橡胶材料的SEM图。从图中可以看出:经过壳寡糖包裹纳米银和氧化石墨烯交替组装后橡胶表面覆盖氧化石墨烯和颗粒状纳米银。
对本实施例抗菌材料进行平板落计数法和抑菌环法测试:
取 100 μL 107 CFU/mL 细菌悬液滴加在抗菌改性橡胶胶片(LMCS-AgNPs/NR 复合材料或 LMCS-AgNPs/GO 自组装膜, 尺寸为 1 cm×1 cm)表面并涂覆均匀,置于 37±1oC、湿度>95 %培养箱内培养 4 h。然后浸泡在盛有 20 mL PBS 缓冲液的小烧杯中,在 37±1 oC 恒温摇床上震荡 10 min,使黏附于胶片表面的细菌洗脱至PBS缓冲液中,并将缓冲液稀释十倍。吸取 60 μL稀释后的 PBS缓冲液均匀涂布到 MH(A)培养基平板上,37±1 oC下培养 24 h,每组重复三次,以未改性天然橡胶胶片为阴性对照组并统计菌落数。并根据菌落数计算抑菌率,计算公式如下:
抑菌率=[(阴性对照组菌落数-试验组菌落数)/阴性对照组菌落数]×100%
试验结果见表1和图2。本实施例制备出的医用橡胶膜片,对金色葡萄球菌和大肠杆菌抑菌率为100%,抑菌环直径为6.8mm和8.4mm。
实施例2
按照实施例1的工艺方法,实施例2的区别在于:交替组装次数为三次。得到含有6层的壳寡糖包裹纳米银为最外层的医用橡胶膜片。试验结果见表1和图2,医用橡胶膜片对金色葡萄球菌和大肠杆菌抑菌率为100%,抑菌环直径为8.2mm和10.2mm。
实施例3
按照实施例1的工艺方法,实施例3的区别在于:交替组装次数为五次。得到含有10层的壳寡糖包裹纳米银为最外层的医用橡胶膜片。试验结果见表1和图2,医用橡胶膜片对金色葡萄球菌和大肠杆菌抑菌率为100%,抑菌环直径为9.0mm和10.9mm。
表1示出了本发明壳寡糖包裹纳米银/氧化石墨烯层层修饰橡胶材料平板菌落计数和抑菌环测试结果。
表1
Figure DEST_PATH_IMAGE001

Claims (6)

1. 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,其特征在于:包括以下步骤:
(1)壳寡糖包裹纳米银的制备
将0.1%wt硝酸银溶液与0.1%wt壳寡糖溶液按体积比为5~30:70~95加入搅拌器中,室温下搅拌0.5-1h,混合溶液置于4mL石英比色皿中,通氮气10s-30s除尽空气并密封,将石英比色皿置于240-290nm紫外灯3-8cm处照射5min-30min,紫外灯功率10-40W;
混合溶液加入相同体积的无水乙醇在13000r/min-15000r/min转速下离心30min-80min取沉淀,并用50%wt乙醇离心洗涤两次并冷冻干燥,即得到壳寡糖包裹纳米银复合抗菌剂CS-AgNPs粉末;壳寡糖包裹纳米银复合抗菌剂粉末溶于水,并超声20-30min,即得壳寡糖包裹纳米银分散液;
(2)天然橡胶NR表面处理
去离子水清洗后的天然橡胶胶片在80%-98%浓硫酸下浸泡5-10min,取出用去离子水清洗3-7次;
(3)在天然橡胶NR表面进行的壳寡糖纳米银和氧化石墨烯层层自组装
将上述步骤(2)得到的天然橡胶基材加入到氧化石墨烯溶液中浸泡30-60min,然后分离出膜片用超纯水溶液洗涤4-6次,制备出表面具有氧化石墨烯的橡胶膜片;再将膜片加入步骤(1)得到的壳寡糖包裹纳米银分散液中浸泡30-60min,分离出膜片用超纯水溶液洗涤4-6次,完成基材表面的第一个双分子层自组装;重复上述过程,在壳寡糖包裹纳米银溶液和氧化石墨烯溶液中分别交替自组装3-5次后,得到壳寡糖包裹纳米银为最外层的表面层层自组装修饰的医用橡胶材料。
2.根据权利要求1所述的壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,其特征在于:所得氧化石墨烯溶液的浓度为0.5-2mg/mL。
3.根据权利要求1所述的壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,其特征在于:所述壳寡糖的分子量为1000-10000。
4.根据权利要求1所述的壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法,其特征在于:所述的氧化石墨烯为微米级,其直径为0.7-1.2 微米,单层氧化石墨烯占总氧化石墨烯的95%以上。
5.一种权利要求1~4任一项所述的壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料的制备方法制得的表面层层自组装修饰的医用橡胶材料。
6.根据权利要求5所述的表面层层自组装修饰的医用橡胶材料,其特征在于:含有2~10层的层状结构。
CN201810144941.0A 2018-02-12 2018-02-12 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法 Active CN108329496B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810144941.0A CN108329496B (zh) 2018-02-12 2018-02-12 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810144941.0A CN108329496B (zh) 2018-02-12 2018-02-12 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法

Publications (2)

Publication Number Publication Date
CN108329496A CN108329496A (zh) 2018-07-27
CN108329496B true CN108329496B (zh) 2021-02-09

Family

ID=62928825

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810144941.0A Active CN108329496B (zh) 2018-02-12 2018-02-12 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法

Country Status (1)

Country Link
CN (1) CN108329496B (zh)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109796753A (zh) * 2019-01-24 2019-05-24 广州大学 一种抗静电抗菌面料母粒及其制备方法
CN109810488A (zh) * 2019-01-25 2019-05-28 厦门美佳美新材料科技有限公司 高耐热氧化石墨烯改性聚碳酸酯塑料粒子及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04231062A (ja) * 1990-09-18 1992-08-19 Create Medic Kk 抗菌性医療用品
CA2636672A1 (en) * 2008-07-17 2010-01-17 Brian Sykora A secure transaction card and electronic device with screen overlay
CN102849730B (zh) * 2012-09-04 2014-12-24 江苏大学 一种制备纳米银-石墨烯仿生纳米结构复合薄膜的方法
CN106417275A (zh) * 2016-08-29 2017-02-22 太原理工大学 壳聚糖包裹纳米银氧化石墨烯复合抗菌材料的制备方法
CN106804624A (zh) * 2017-01-15 2017-06-09 华东理工大学 一种纳米壳寡糖/银复合诱导抗菌材料的制备方法

Also Published As

Publication number Publication date
CN108329496A (zh) 2018-07-27

Similar Documents

Publication Publication Date Title
Mallakpour et al. State-of-the-art of 3D printing technology of alginate-based hydrogels—An emerging technique for industrial applications
Zhong et al. Titanium surface priming with phase-transited lysozyme to establish a silver nanoparticle-loaded chitosan/hyaluronic acid antibacterial multilayer via layer-by-layer self-assembly
Agnihotri et al. Development of nano-antimicrobial biomaterials for biomedical applications
Lakshman et al. Preparation of silver nanoparticles incorporated electrospun polyurethane nano-fibrous mat for wound dressing
EP1657980B1 (en) Anti-virus hydrophilic polymeric material
Noorisafa et al. Surface modification of polyurethane via creating a biocompatible superhydrophilic nanostructured layer: role of surface chemistry and structure
CN106620900B (zh) 一种基于仿生多巴胺原位还原纳米银的多层膜长效抗菌涂层的制备方法
Redfern et al. Toxicity and antimicrobial properties of ZnO@ ZIF-8 embedded silicone against planktonic and biofilm catheter-associated pathogens
CN108329496B (zh) 一种壳寡糖纳米银/氧化石墨烯修饰的医用橡胶材料及其制备方法
CN101151967A (zh) 以贝壳粉为载体的纳米抗菌粉体及其制备方法
Dobosz et al. Green materials science and engineering reduces biofouling: approaches for medical and membrane-based technologies
Abu-Saied et al. Polyvinyl alcohol/Sodium alginate integrated silver nanoparticles as probable solution for decontamination of microbes contaminated water
CN104740690B (zh) 一种海洋生物载药纳米抗菌超滑涂层
Zang et al. Metal–organic framework polymer coating inhibits Staphylococcus aureus attachment on medical circulation tubing under static and dynamic flow conditions
CN114392388A (zh) 一种水凝胶组合物及其应用
Wang et al. A homogeneous dopamine–silver nanocomposite coating: striking a balance between the antibacterial ability and cytocompatibility of dental implants
CN108118444A (zh) 一种纳米银抗菌纤维膜的制备方法
Liu et al. Fabrication of a bionic asymmetric wettable Cu-doped chitosan-laponite-PCL wound dressing with rapid healing and antibacterial effect
CN103933617B (zh) 一种具有抗细菌粘附的气管导管的制备方法
Haugen et al. Antibacterial effects of titanium dioxide in wounds
US20080139998A1 (en) Breastpump Assemblies Having Silver-Containing Antimicrobial Compounds
CN109122678A (zh) 一种纳米银负载于两亲性生物碳材料的纳米银复合物及其制法和用途
KR20120112968A (ko) 아파타이트를 복합한 항균성 폴리우레탄 필름의 제조방법
CN111494603A (zh) 一种抗菌肽纳米软膏及其制备方法和用途
CN101838455B (zh) 香菇多糖硫酸酯与纳米银自组装修饰的聚氨酯材料及制备

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant